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LidoCream 10

Medically reviewed by Drugs.com. Last updated on Nov 1, 2021.

Dosage form: cream
Ingredients: LIDOCAINE 10g in 100g
Labeler: Golden Touch LLC
NDC Code: 52763-101

LidoCream 10

Drug Facts

Active Ingredient

Lidocaine 10% w/w

Purpose

Topical Anesthetic

Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.

Uses For the temporary relief of pain and itching due to anorectal disorders

Warnings

For external use only

When using this product • avoid contact with eyes • do not put in rectum • do not exceed recommended dosage unless directed by a doctor

Stop use and ask a doctor if: • allergic reaction occurs • condition worsens or does not improve within 7 days • symptoms clear up and return within a few days • rectal bleeding occurs • redness, irritation, swelling, pain or other symptoms develop or increase

Directions • Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly • Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product • Apply externally to the affected area upto 6 times daily • Children under 12 years of age: consult a doctor

Inactive Ingredients Aloe Barbadensis Leaf Extract, Benzyl Alcohol, Carbomer, Disodium EDTA, Glycerin, Glyceryl Monooleate, SD Alcohol 40-B, Simmondsia Chinensis (Jojoba) Seed Oil, Water.

Packaging

LIDOCREAM 10 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52763-101
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (LIDOCAINE) LIDOCAINE10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
BENZYL ALCOHOL 
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) 
EDETATE DISODIUM 
GLYCERIN 
GLYCERYL OLEATE 
ALCOHOL 
SIMMONDSIA CHINENSIS SEED 
WATER 
Packaging
#Item CodePackage Description
1NDC:52763-101-601 TUBE in 1 CARTON
160 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34605/05/2015
Labeler - Golden Touch LLC (194284147)
Establishment
NameAddressID/FEIOperations
Golden Touch LLC194284147manufacture(52763-101)

 
Golden Touch LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.